Efficacy and Safety of Avatrombopag in Cancer Patients With Thrombocytopenia

Thrombocytopenia Clinical Trial

Official title: Efficacy and Safety of Avatrombopag in Cancer Patients With Thrombocytopenia Induced by Targeted Therapy and Immunotherapy Combination Treatment

Status Recruiting

Clinical Trial Summary

To evaluate the efficacy and safety of Avatrombopag in patients with thrombocytopenia induced by targeted therapy and immunotherapy combination treatment, and provide evidence-based medication for the clinical use of Avatrombopag in patients with PC ≤50×109/L

Clinical Trial Description

This phase II trial is a single-arm, non-randomized and single-center clinical study.

It is estimated that 30 patients who met the study criteria will be enrolled in PUMCH and treated with Avatrombopag. The investigators will follow up and collect subjects' data each month to evaluate the efficacy and safety of treatment. Primary outcome measure is percentage of participants whose PLT reaches ≥75×109/L, or increases by ≥50×109/L or ≥100% from baseline at least once within 20 days of initial treatment.

Secondary outcome measure:1)Number of days required for PLT to reach ≥50×109/L after treatment; 2)Number of days required for PLT to reach ≥75×109/L after treatment; 3)Percentage of subjects without platelet transfusion within 20 days of treatment; 4)Percentage of subjects without clinically relevant bleeding within 20 days of treatment.

Study Type: Interventional. Masking: Open Label. ;

Related Conditions & MeSH terms

• Thrombocytopenia

• NCT number: NCT04896528
• Study type: Interventional
• Source: Peking Union Medical College Hospital
• Contact: Yanyu Wang, MD
• Phone: +86 15810784518
• Email: pumcwyy950105@163.com
• Status: Recruiting
• Phase: Phase 2
• Start date: June 6, 2021
• Completion date: December 31, 2021